Engineer I - 2º Shift

Amgen

Us
Base: 88,281.00usd - 119,439.00usd; bonus/equity: ...
On-site
Biopharmaceutical process equipment ownership
Gmp compliance and regulatory interaction
Root cause analysis and problem solving
Amgen is seeking an Engineer I for their 2nd shift operations, focusing on downstream process engineering within their Facilities & Engineering group. The role entails system ownership, process improvements, and collaboration with various teams to ensure reliable plant operations

Job Summary

  • Join Amgen's mission to serve patients living with serious illnesses by pioneering the world of biotech.
  • This role will develop domain expertise and system ownership to support process operations, focusing on Downstream Process engineering.
  • Amgen offers a comprehensive employee benefits package, a discretionary annual bonus program, and stock-based long-term incentives.

Matching Summary

Match Score: 85

Amgen is seeking an Engineer I for their 2nd shift operations, focusing on downstream process engineering within their Facilities & Engineering group. The role entails system ownership, process improvements, and collaboration with various teams to ensure reliable plant operations.

Salary

Base: 88,281.00USD - 119,439.00USD; Bonus/Equity: Discretionary annual bonus program, Stock-based long-term incentives; Benefits: Comprehensive employee benefits package

Skills & Requirements

Must-have

  • Biopharmaceutical process equipment ownership
  • GMP compliance and regulatory interaction
  • Root cause analysis and problem solving
  • Cross-functional collaboration

Nice-to-have

  • Proactive risk reduction strategies
  • New product/technology introduction support
  • Collaborative team-based environment

Key Requirements

  • 8 years Engineering/Maintenance experience with High school diploma/GED
  • 6 years Engineering/Maintenance experience with Associate’s degree
  • 2 years Engineering/Maintenance experience with Bachelor’s degree
  • Master’s degree
  • Bachelor’s degree in Chemical or Mechanical engineering preferred
  • Experience with GMP Biopharmaceutical Production facility equipment/systems
  • Experience in regulated environments (cGMP, OSHA, EPA)
  • Work schedule flexibility for 24/7 operations

Work Rights

Not specified

Tailored Resume

Cover Letter